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Coenzyme A
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#	Item
91	PRENATAL DIAGNOSIS Prenat Diagn 2001; 21: 52±54. INVITED COMMENTARY: CURRENT ISSUES IN OBSTETRICS AND GENETICS Add to Reading List Source URL: www.fodsupport.org Language: English - Date: 2012-05-31 13:41:15 Medicine Coenzymes Fatty acids Inborn error of lipid metabolism Fatty-acid metabolism disorder Fatty acid metabolism Long-chain 3-hydroxyacyl-coenzyme A dehydrogenase deficiency Carnitine Very long-chain acyl-coenzyme A dehydrogenase deficiency Biology Chemistry Metabolism
92	Fatty acid oxidation is important for immune cell function: The NIH MINI Study receives additional funding to study immune function Add to Reading List Source URL: www.fodsupport.org Language: English - Date: 2014-07-23 04:41:27 Immunology Fatty acids Very long-chain acyl-coenzyme A dehydrogenase deficiency Lipid Metabolism Carnitine palmitoyltransferase I T cells Immune system Fatty-acid metabolism disorder Medicine Health Biology
93	EXPANDED NEWBORN SCREENING 2005 to 2009 MISSED OPPORTUNITIES -- POTENTIAL LEGAL CLAIMS Over the past five years, it’s become clear that many children who should have had the benefit of expanded screening did not. By ea Add to Reading List Source URL: fodsupport.org Language: English - Date: 2012-05-31 13:41:05 Medical genetics Newborn screening Propionic acidemia Methylmalonic acidemia Isovaleric acidemia Very long-chain acyl-coenzyme A dehydrogenase deficiency Glutaric aciduria type 1 Malonyl-CoA decarboxylase deficiency Medium-chain acyl-coenzyme A dehydrogenase deficiency Health Rare diseases Genetic genealogy
94	Tri-Functional Protein (TFP) Deficiency (metabolic condition: fatty acid oxidation disorder) Also known as: • mitochondrial trifunctional protein deficiency • trifunctional enzyme deficiency Add to Reading List Source URL: www.albertahealthservices.ca Language: English - Date: 2013-09-16 18:36:24 Fatty acids Mitochondrial trifunctional protein deficiency Fatty-acid metabolism disorder Hepatology Long-chain 3-hydroxyacyl-coenzyme A dehydrogenase deficiency Mitochondrial trifunctional protein 3-hydroxyacyl-coenzyme A dehydrogenase deficiency Fatty acid metabolism Medical genetics Medicine Health Rare diseases
95	Microsoft Word - Incidence_Table_2013_rev.doc Add to Reading List Source URL: health.hawaii.gov Language: English - Date: 2013-05-30 19:58:49 Genetic genealogy Pediatrics Epidemiology Newborn screening Adrenal gland disorders Intersexuality Isovaleric acidemia Maple syrup urine disease Medium-chain acyl-coenzyme A dehydrogenase deficiency Health Medicine Rare diseases
96	MISSION FOD FAMILY SUPPORT GROUP Deb Lee Gould, MEd, Director ♥ CREATE AWARENESS & EDUCATE the Public & Professionals about Fatty Oxidation Add to Reading List Source URL: fodsupport.org Language: English - Date: 2012-05-31 13:40:54 Biology Fatty-acid metabolism disorder Newborn screening Carnitine-acylcarnitine translocase deficiency Carnitine-acylcarnitine translocase Very long-chain acyl-coenzyme A dehydrogenase deficiency Carnitine Long-chain 3-hydroxyacyl-coenzyme A dehydrogenase deficiency Systemic primary carnitine deficiency Health Medicine Rare diseases
97	BinderE for SJC Sept05.p65 Add to Reading List Source URL: www.cpsp.cps.ca Language: English - Date: 2012-10-22 14:28:32 Medium-chain acyl-coenzyme A dehydrogenase deficiency Newborn screening Fatty-acid metabolism disorder ACADM Hypoglycemia Acute fatty liver of pregnancy Carnitine Inborn error of lipid metabolism Health Medicine Pediatrics
98	MEDIUM CHAIN ACYL-COENZYME A DEHYDROGENASE DEFICIENCY (MCADD) Add to Reading List Source URL: www.cpsp.cps.ca Language: English - Date: 2012-10-22 14:28:39 Pediatrics Kernicterus Neonatal jaundice Jaundice Athetosis Bilirubin Glucose-6-phosphate dehydrogenase deficiency Pantothenate kinase-associated neurodegeneration Hereditary spherocytosis Medicine Health Hepatology
99	Deb Lee Gould, MEd, Director MCAD Parent and Grief Consultant Grief Support for Bereaved Parents and Families FOD Add to Reading List Source URL: www.fodsupport.org Language: English - Date: 2013-01-08 08:30:02 Medium-chain acyl-coenzyme A dehydrogenase deficiency Carnitine Fatty-acid metabolism disorder Newborn screening Health Medicine Chemistry
100	Maine Newborn Screening Program List of Conditions Each baby born in Maine is screened for the conditions listed below. This list is correct as of July 1, 2008 but may change as conditions are added to or removed from th Add to Reading List Source URL: www.maine.gov Language: English - Date: 2011-11-10 05:38:14 Medical genetics Newborn screening Hyperammonemia 3-Methylcrotonyl-CoA carboxylase deficiency Isovaleric acidemia Glutaric acidemia type 2 Glutaric aciduria type 1 Propionic acidemia Long-chain 3-hydroxyacyl-coenzyme A dehydrogenase deficiency Health Rare diseases Genetic genealogy

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